Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP342946.RAoTG6rFfLjkQ8zlI9_DtpqLl2KXA9Ps6YN-rOE2HBCT4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP342946.RAoTG6rFfLjkQ8zlI9_DtpqLl2KXA9Ps6YN-rOE2HBCT4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP342946.RAoTG6rFfLjkQ8zlI9_DtpqLl2KXA9Ps6YN-rOE2HBCT4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP342946.RAoTG6rFfLjkQ8zlI9_DtpqLl2KXA9Ps6YN-rOE2HBCT4130_provenance.
- NP342946.RAoTG6rFfLjkQ8zlI9_DtpqLl2KXA9Ps6YN-rOE2HBCT4130_assertion description "[Using microsatellite analysis, Southern blot analysis, and fluorescence in situ hybridization (FISH), 30 primary tumors and six CSF metastasis specimens were analyzed for loss of heterozygosity (LOH) of chromosomes 1q31, 6q, 9q22, 10q, 11, 16q22, and 17p13.1 and/or high-level amplification of the c-myc gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP342946.RAoTG6rFfLjkQ8zlI9_DtpqLl2KXA9Ps6YN-rOE2HBCT4130_provenance.
- NP342946.RAoTG6rFfLjkQ8zlI9_DtpqLl2KXA9Ps6YN-rOE2HBCT4130_assertion evidence source_evidence_literature NP342946.RAoTG6rFfLjkQ8zlI9_DtpqLl2KXA9Ps6YN-rOE2HBCT4130_provenance.
- NP342946.RAoTG6rFfLjkQ8zlI9_DtpqLl2KXA9Ps6YN-rOE2HBCT4130_assertion SIO_000772 9667267 NP342946.RAoTG6rFfLjkQ8zlI9_DtpqLl2KXA9Ps6YN-rOE2HBCT4130_provenance.
- NP342946.RAoTG6rFfLjkQ8zlI9_DtpqLl2KXA9Ps6YN-rOE2HBCT4130_assertion wasDerivedFrom befree-20140225 NP342946.RAoTG6rFfLjkQ8zlI9_DtpqLl2KXA9Ps6YN-rOE2HBCT4130_provenance.
- NP342946.RAoTG6rFfLjkQ8zlI9_DtpqLl2KXA9Ps6YN-rOE2HBCT4130_assertion wasGeneratedBy ECO_0000203 NP342946.RAoTG6rFfLjkQ8zlI9_DtpqLl2KXA9Ps6YN-rOE2HBCT4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP342946.RAoTG6rFfLjkQ8zlI9_DtpqLl2KXA9Ps6YN-rOE2HBCT4130_provenance.